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159 related items for PubMed ID: 12228913
1. Fluorescent in situ hybridization (FISH) reveals frequent and recurrent numerical and structural abnormalities in hepatoblastoma with no informative karyotype. Surace C, Leszl A, Perilongo G, Rocchi M, Basso G, Sainati L. Med Pediatr Oncol; 2002 Nov; 39(5):536-9. PubMed ID: 12228913 [Abstract] [Full Text] [Related]
3. Cytogenetic evaluation of a large series of hepatoblastomas: numerical abnormalities with recurring aberrations involving 1q12-q21. Tomlinson GE, Douglass EC, Pollock BH, Finegold MJ, Schneider NR. Genes Chromosomes Cancer; 2005 Oct; 44(2):177-84. PubMed ID: 15981236 [Abstract] [Full Text] [Related]
4. Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study. Parada LA, Limon J, Iliszko M, Czauderna P, Gisselsson D, Höglund M, Kullendorff CM, Wiebe T, Mertens F, Johansson B. Med Pediatr Oncol; 2000 Mar; 34(3):165-70. PubMed ID: 10696121 [Abstract] [Full Text] [Related]
7. [Cytogenetic study of 121 patients suffering from various hematologic neoplasms using the in situ hybridization technique]. Pérez Losada A, Solé F, Woessner S, Florensa L, Besses C, Espinet B, Caballín MR, García Eroles L, Sans-Sabrafén J. Sangre (Barc); 1996 Jun; 41(3):201-9. PubMed ID: 8755208 [Abstract] [Full Text] [Related]
10. Trisomy 1q, 2, and 20 in a case of hepatoblastoma: possible significance of 2q35-q37 and 1q12-q21 rearrangements. Yeh YA, Rao PH, Cigna CT, Middlesworth W, Lefkowitch JH, Murty VV. Cancer Genet Cytogenet; 2000 Dec; 123(2):140-3. PubMed ID: 11150606 [Abstract] [Full Text] [Related]
11. [Detection of numerical chromosomal aberrations in hematopoietic malignancy by in situ hybridization on bone marrow aspirate paraffin sections]. Okada T, Noriki S, Maekawa H, Mori M, Torii K, Ichikawa M, Gejyo F. Rinsho Byori; 1996 Dec; 44(12):1175-82. PubMed ID: 8990937 [Abstract] [Full Text] [Related]
12. Hidden chromosome 8 abnormalities detected by FISH in adult primary myelodysplastic syndromes. Panani AD, Pappa V. In Vivo; 2005 Dec; 19(6):979-81. PubMed ID: 16277010 [Abstract] [Full Text] [Related]
13. [2q21-qter trisomy in hepatoblastoma]. Balogh E, Swanton S, Kiss C, Jakab Z, Secker-Walker LM, Oláh E. Orv Hetil; 1997 Dec 14; 138(50):3179-83. PubMed ID: 9446083 [Abstract] [Full Text] [Related]
15. Combined cytogenetic testing and fluorescence in situ hybridization analysis in the study of chronic lymphocytic leukemia and multiple myeloma. Wiktor A, Van Dyke DL. Cancer Genet Cytogenet; 2004 Aug 14; 153(1):73-6. PubMed ID: 15325099 [Abstract] [Full Text] [Related]
16. Hepatoblastoma in a child with trisomy 18: cytogenetics, liver anomalies, and literature review. Bove KE, Soukup S, Ballard ET, Ryckman F. Pediatr Pathol Lab Med; 1996 Aug 14; 16(2):253-62. PubMed ID: 9025831 [Abstract] [Full Text] [Related]
17. Fluorescence in situ hybridization analysis of aneuploidization patterns in monoclonal gammopathy of undetermined significance versus multiple myeloma and plasma cell leukemia. Rasillo A, Tabernero MD, Sánchez ML, Pérez de Andrés M, Martín Ayuso M, Hernández J, Moro MJ, Fernández-Calvo J, Sayagués JM, Bortoluci A, San Miguel JF, Orfao A. Cancer; 2003 Feb 01; 97(3):601-9. PubMed ID: 12548602 [Abstract] [Full Text] [Related]